Potential vascular α-adrenoceptor blocking properties of metformin in rat aorta and tail artery.

Eur J Pharmacol

Departamento de Farmacobiología, Cinvestav Unidad Coapa, Czda. de los Tenorios 235, Col. Granjas-Coapa, Del. Tlalpan, C.P. 14330, D.F, Mexico. Electronic address:

Published: September 2019

AI Article Synopsis

  • Metformin is a common medication for type 2 diabetes that may also lower blood pressure, though the exact mechanism through α-adrenoceptors needs more research.
  • The study tested metformin's effects on rat aorta and tail artery contractions caused by noradrenaline, methoxamine, and phenylephrine.
  • Results indicated that metformin effectively blocked these contractions at different concentrations, supporting the idea that its ability to block α-adrenoceptors could contribute to its blood pressure-lowering effects observed in clinical settings.

Article Abstract

Metformin is a widely used drug for the treatment of type 2 Diabetes Mellitus. Several studies have also suggested that metformin decreases blood pressure; although an interaction with α-adrenoceptors has been proposed, this mechanism needs to be further investigated. Since α-adrenoceptors play a significant role to regulate vascular tone, this study has analysed the potential ability of metformin to block α-adrenoceptors in rat aorta and tail artery. For this purpose, the contractile responses induced by noradrenaline, methoxamine, and phenylephrine were determined in the absence or presence of metformin in rat aorta and tail artery rings. In both arteries, noradrenaline, methoxamine, and phenylephrine produced concentration-dependent contractile responses. Interestingly, the contractile responses to noradrenaline, methoxamine, and phenylephrine were significantly and differentially blocked by metformin (1, 3.1 and/or 10 mM) but not by vehicle. These results suggest that metformin is capable to block α-adrenoceptors and may explain, at least in part, the anti-hypertensive effect observed in several clinical trials.

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http://dx.doi.org/10.1016/j.ejphar.2019.172498DOI Listing

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